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In-depth transcriptomic analyses of LncRNA and mRNA expression in the hippocampus of APP/PS1 mice by Danggui-Shaoyao-San

机译:Danggui-Shaoyao-SAN的APP / PS1小鼠海马LNCRNA和mRNA表达的深入转录组分析

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摘要

Alzheimer’s disease (AD) is an age-related neurodegenerative disease with a high incidence worldwide, and with no medications currently able to prevent the progression of AD. Danggui-Shaoyao-San (DSS) is widely used in traditional Chinese medicine (TCM) and has been proven to be effective for memory and cognitive dysfunction, yet its precise mechanism remains to be delineated. The present study was designed to investigate the genome-wide expression profile of long non-coding RNAs (LncRNAs) and messenger RNAs (mRNAs) in the hippocampus of APP/PS1 mice after DSS treatment by RNA sequencing. A total of 285 differentially expressed LncRNAs and 137 differentially expressed mRNAs were identified (fold-change ≥2.0 and P < 0.05). Partial differentially expressed LncRNAs and mRNAs were selected to verify the RNA sequencing results by quantitative polymerase chain reaction (qPCR). A co-expression network was established to analyze co-expressed LncRNAs and genes. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were used to evaluate the biological functions related to the differentially co-expressed LncRNAs, and the results showed that the co-expressed LncRNAs were mainly involved in AD development from distinct origins, such as APP processing, neuron migration, and synaptic transmission. Our research describes the lncRNA and mRNA expression profiles and functional networks involved in the therapeutic effect of DSS in APP/PS1 mice model. The results suggest that the therapeutic effect of DSS on AD involves the expression of LncRNAs. Our findings provide a new perspective for research on the treatment of complex diseases using traditional Chinese medicine prescriptions.
机译:阿尔茨海默病的疾病(AD)是一种与全世界发病率高的年龄相关的神经变性疾病,目前没有任何药物能够防止广告进展。 Danggui-Shaoyao-San(DSS)广泛用于中药(TCM),已被证明对内存和认知功能障碍有效,但其精确的机制仍有缺陷。设计本研究旨在在通过RNA测序处理的DSS处理后,研究在APP / PS1小鼠的海马中长的非编码RNA(LNCRNA)和信使RNA(MRNA)的基因组表达谱。鉴定了总共285例差异表达的LNCRNA和137个差异表达的MRNA(折叠变化≥2.0和P <0.05)。选择局部差异表达的LNCRNA和MRNA以通过定量聚合酶链反应(QPCR)来验证RNA测序结果。建立了一种共表达网络,分析了共同表达的LNCRNA和基因。基因本体(GO)和京都基因和基因组(KEGG)分析用于评估与差异共同表达的LNCRNA相关的生物学功能,结果表明,共表达的LNCRNA主要涉及不同的广告发展起源,如应用处理,神经元迁移和突触传输。我们的研究描述了在APP / PS1小鼠模型中DSS的治疗效果中的LNCRNA和mRNA表达谱和功能网络。结果表明,DSS对AD的治疗效果涉及LNCRNA的表达。我们的调查结果为使用中医处方进行了研究的复杂疾病的研究提供了一种新的视角。

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